Solid state synthesis, characterization, optical properties and cooperative catalytic performance of bismuth vanadate nanocatalyst for Biginelli reactions

RSC Advances ◽  
2015 ◽  
Vol 5 (31) ◽  
pp. 24313-24318 ◽  
Author(s):  
Shahin Khademinia ◽  
Mahdi Behzad ◽  
Hamideh Samari Jahromi

Bi2V2O7 nano powders were synthesized via a solid state reaction at 500 °C for 8 h using Bi(NO3)3 and VO(acac)2 at stoichiometric 1 : 1 Bi : V molar ratio as raw materials.

2012 ◽  
Vol 534 ◽  
pp. 110-113 ◽  
Author(s):  
Fei Shi ◽  
Peng Cheng Du ◽  
Jing Xiao Liu ◽  
Ji Wei Wu ◽  
Chun Yuan Luo

Using basic magnesium carbonate (Mg(OH)2•4MgCO3•6H2O) and SiO2 as raw materials, forsterite (Mg2SiO4) was prepared by solid state synthesis process. The optimal process for synthesizing Mg2SiO4 was obtained by adjusting Mg/Si molar ratio and sintering temperature. The crystal phase of the obtained Mg2SiO4 powder was determined by X-ray diffraction (XRD). The results indicate that the single-phase Mg2SiO4 powder can be obtained when the mixtures with Mg/Si molar ratio of 2.05~2.01 were sintered at 1350°C for 3h in the air. The as-prepared Mg2SiO4 ceramic samples which were sintered at 1300~1360°C showed better dielectric properties with εr=7.4 and tanδ =7.5×10-4.


2008 ◽  
Vol 368-372 ◽  
pp. 683-685
Author(s):  
Cheng Wei Hao ◽  
Bo Lin Wu ◽  
Ji Yan Li

Ammonium aluminium carbonate hydroxide (AACH), with a small quantity of γ-AlOOH, was synthesized through solid-state reaction at room temperature using AlCl3·6H2O and NH4HCO3 as raw materials and polyethylene glycol (PEG-10000) as the dispersant. After calcined at 1100°C for 1.5h, α-Al2O3 powders with primary particle sizes of 20~30nm were obtained. The crystal phase, particle size and morphology of the high-purity ultrafine α-Al2O3 were characterized. The results showed that a small quantity of γ-AlOOH in the AACH decomposed and formed crystal seeds. The presence of crystal seeds reduced the nucleation activation energy and therefore reduced the phase transformation temperature.


2013 ◽  
Vol 581 ◽  
pp. 101-108 ◽  
Author(s):  
Z. Kotan ◽  
M. Ayvacikli ◽  
Y. Karabulut ◽  
J. Garcia-Guinea ◽  
L. Tormo ◽  
...  

2019 ◽  
Vol 55 (6) ◽  
pp. 2291-2302 ◽  
Author(s):  
A. Jalalian-Khakshour ◽  
C. O. Phillips ◽  
L. Jackson ◽  
T. O. Dunlop ◽  
S. Margadonna ◽  
...  

Abstract In this work, the effect of varying the size of the precursor raw materials SiO2 and ZrO2 in the solid-state synthesis of NASICON in the form Na3Zr2Si2PO12 was studied. Nanoscale and macro-scale precursor materials were selected for comparison purposes, and a range of sintering times were examined (10, 24 and 40 h) at a temperature of 1230 °C. Na3Zr2Si2PO12 pellets produced from nanopowder precursors were found to produce substantially higher ionic conductivities, with improved morphology and higher density than those produced from larger micron-scaled precursors. The nanoparticle precursors were shown to give a maximum ionic conductivity of 1.16 × 10−3 S cm−1 when sintered at 1230 °C for 40 h, in the higher range of published solid-state Na3Zr2Si2PO12 conductivities. The macro-precursors gave lower ionic conductivity of 0.62 × 10−3 S cm−1 under the same processing conditions. Most current authors do not quote or consider the precursor particle size for solid-state synthesis of Na3Zr2Si2PO12. This study shows the importance of precursor powder particle size in the microstructure and performance of Na3Zr2Si2PO12 during solid-state synthesis and offers a route to improved predictability and consistency of the manufacturing process.


RSC Advances ◽  
2018 ◽  
Vol 8 (28) ◽  
pp. 15613-15620 ◽  
Author(s):  
Xiaochun He ◽  
Ruiqing Chu ◽  
Zhijun Xu ◽  
Zhongran Yao ◽  
Jigong Hao

Lead-free ceramics, SrBi2Nb2O9–xBi2O3 (SBN–xBi), with different Bi contents of which the molar ratio, n(Sr) : n(Bi) : n(Nb), is 1 : 2(1 + x/2) : 2 (x = −0.05, 0.0, 0.05, 0.10), were prepared by conventional solid-state reaction method.


2014 ◽  
Vol 6 (2) ◽  
pp. 217-231 ◽  
Author(s):  
F. Khatun ◽  
M. A. Gafur ◽  
M. S. Ali ◽  
M. S. Islam ◽  
M. A. R. Sarker

The lithium-cobalt oxide LixCoO2 is a promising candidate as highly active cathode material of lithium ion rechargeable batteries. The crystalline-layered lithium cobaltite has attracted increased attention due to recent discoveries of some extraordinary properties such as unconventional transport and magnetic properties. Due to layered crystal structure, Li contents (x) in LixCoO2 might play an important role on its interesting properties. LiCoO2 crystalline cathode material was prepared by using solid-state reaction synthesis, and then LixCoO2 (x<1) has been synthesized by deintercalation of produced single-phase powders. Structure and morphology of the synthesized powders were investigated by X-ray diffraction (XRD), Infrared spectroscopy, Impedance analyzer etc. The influence of lithium composition (x) on structural, electronic and optical properties of lithium cobaltite was studied. Temperature dependent electrical resistivity was measured using four-probe technique. While LixCoO2 with x = 0.9 is a semiconductor, the highly Li-deficient phase (0.75 ? x ? 0.5) exhibits metallic conductivity. The ionic conductivity of LixCoO2 (x = 0.5 – 1.15) was measured using impedance spectroscopy and maximum conductivity of Li0.5CoO2 was found to be 6.5×10-6 S/cm at 273 K. The properties that are important for applications, such as ionic conductivity, charge capacity, and optical absorption are observed to increase with Li deficiency. Keywords: Calcination; Characterization; Inorganic compounds; Solid-State reaction; X-ray diffraction. © 2014 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved.doi: http://dx.doi.org/10.3329/jsr.v6i2.17900 J. Sci. Res. 6 (2), 217-231 (2014)  


Sign in / Sign up

Export Citation Format

Share Document